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98645-45-5

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98645-45-5 Usage

General Description

2-chloro-4-ethoxynicotinonitrile is a chemical compound with the molecular formula C9H8ClNO and a molecular weight of 173.62 g/mol. It is a nitrile derivative of 2-chloro-4-ethoxypyridine and is widely used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 2-chloro-4-ethoxynicotinonitrile is a white solid with a melting point of around 87-89°C and is sparingly soluble in water. It is primarily utilized in the production of nicotinoyl chloride, which is an important building block for the synthesis of various organic compounds. Additionally, 2-chloro-4-ethoxynicotinonitrile is utilized in the preparation of insecticides and herbicides due to its pesticidal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 98645-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98645-45:
(7*9)+(6*8)+(5*6)+(4*4)+(3*5)+(2*4)+(1*5)=185
185 % 10 = 5
So 98645-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2O/c1-2-12-7-3-4-11-8(9)6(7)5-10/h3-4H,2H2,1H3

98645-45-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-ethoxypyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-chloro-4-ethoxy-pyridine-3-carbonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:98645-45-5 SDS

98645-45-5Relevant articles and documents

An efficient method for the preparation of 4-alkoxy-substituted thieno[2,3-b]pyridines

Saito, Keiji,Naito, Satoru,Shinozuka, Tsuyoshi

, p. 1491 - 1501 (2014/07/07)

An efficient method for the preparation of 4-alkoxy-substituted thieno[2,3-b]pyridines is described. The key intermediates, 4-alkoxy-2-chloro-3- cyanopyridines, were synthesized from a variety of alcohols by nucleophilic substitution with 3-cyano-2,4-dich

THIENOPYRIDINE DERIVATIVES

-

Page/Page column 142, (2010/11/26)

The present invention provides a compound promoting osteogenesis. The present invention provides a compound having the following general formula (I) wherein R 1 is H or alkyl, R 2 is R a S-, R a O-, R a NH-, R a (R b )N- or cyclic amino, and R a and R b are alkyl which may be substituted, cycloalkyl which may be substituted, or the like, or a pharmacologically acceptable salt thereof.

Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists

Zheng, Guo Zhu,Bhatia, Pramila,Daanen, Jerome,Kolasa, Teodozyj,Patel, Meena,Latshaw, Steven,El Kouhen, Odile F.,Chang, Renjie,Uchic, Marie E.,Miller, Loan,Nakane, Masaki,Lehto, Sonya G.,Honore, Marie P.,Moreland, Robert B.,Brioni, Jorge D.,Stewart, Andrew O.

, p. 7374 - 7388 (2007/10/03)

SAR (structure-activity relationship) studies of triazafluorenone derivatives as potent mGluR1 antagonists are described. The triazafluorenone derivatives are non-amino acid derivatives and noncompetitive mGluR1 antagonists that bind at a putative alloste

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